Clinical Research Coordinator

Responsibilities Develops and executes country-level site engagement strategies aligned with internal priorities. Conducts early, strategic landscaping and site engagement (in-person or remote). Builds deep, multi-stakeholder relationships at strategic sites. Serves as the local escalation point for study challenges. Partners seamlessly with internal teams and CROs to ensure unified site communication. Manages assigned local/global clinical studies by overseeing CRO performance. Focus on driving adoption of DCT and digital solutions with our sites. Requirements Degree (MD, PhD, MA / MS, BA / BS) in life sciences or equivalent. Minimum 5+ years of relevant clinical research or clinical operations experience in pharmaceutical, biotech or related industry; Sponsor experience preferred. Experience in end-to-end product development and expert understanding of ICH/GCP are both essential. Understanding of end-to-end clinical trial processes, including monitoring, and strong knowledge of clinical trial regulations and guidelines. Proven track record in managing site relationships and overseeing complex clinical trials. Exceptional interpersonal, cross-functional, negotiation, and influencing skills with a proven track record of building high-trust, sustainable relationships with internal stakeholders, CROs, and site personnel. Ability and willingness to travel domestically between 30-50% dependent on business or site needs. #J-18808-Ljbffr